Variant report

Variant	nsv514221
Chromosome Location	chr4:68793517-68833125
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr4:68799641-68799825	K562	blood:	n/a	n/a
2	ATF1	chr4:68794343-68794570	K562	blood:	n/a	n/a
3	BACH1	chr4:68794347-68794496	H1-hESC	embryonic stem cell:	n/a	n/a
4	BRCA1	chr4:68795302-68795527	Hela-S3	cervix:	n/a	n/a
5	CEBPB	chr4:68794274-68794457	K562	blood:	n/a	n/a
6	CEBPB	chr4:68794296-68794614	Hela-S3	cervix:	n/a	n/a
7	CEBPB	chr4:68813237-68813501	HepG2	liver:	n/a	chr4:68813348-68813359
8	CEBPB	chr4:68794230-68794706	MCF-7	breast:	n/a	n/a
9	CEBPB	chr4:68795056-68795621	HCT-116	colon:	n/a	n/a
10	CEBPB	chr4:68795096-68795523	Hela-S3	cervix:	n/a	n/a
11	CTCF	chr4:68823280-68823333	GM10266	blood:	n/a	n/a
12	CTCF	chr4:68794585-68794605	K562	blood:	n/a	n/a
13	CTCF	chr4:68819804-68819825	LNCaP	prostate:	n/a	n/a
14	CTCF	chr4:68802980-68803130	GM06990	blood:	n/a	n/a
15	E2F4	chr4:68809655-68809657	MCF10A-Er-Src	breast:	n/a	n/a
16	E2F4	chr4:68795165-68795377	MCF10A-Er-Src	breast:	n/a	n/a
17	EP300	chr4:68795219-68795500	SK-N-SH_RA	brain:	n/a	n/a
18	EP300	chr4:68795138-68795510	Hela-S3	cervix:	n/a	n/a
19	EP300	chr4:68794220-68794884	MCF-7	breast:	n/a	n/a
20	EP300	chr4:68795229-68795494	SK-N-SH_RA	brain:	n/a	n/a
21	EP300	chr4:68794245-68794728	MCF-7	breast:	n/a	n/a
22	ESR1	chr4:68794389-68794607	T-47D	breast:	n/a	chr4:68794515-68794532 chr4:68794516-68794531 chr4:68794496-68794511
23	ESR1	chr4:68794354-68794677	T-47D	breast:	n/a	chr4:68794515-68794532 chr4:68794516-68794531 chr4:68794496-68794511
24	ESR1	chr4:68794370-68794707	T-47D	breast:	n/a	chr4:68794515-68794532 chr4:68794516-68794531 chr4:68794496-68794511
25	FOS	chr4:68794333-68794503	MCF10A-Er-Src	breast:	n/a	n/a
26	FOS	chr4:68796964-68797173	MCF10A-Er-Src	breast:	n/a	chr4:68797085-68797092 chr4:68797084-68797093 chr4:68797084-68797092 chr4:68797083-68797092
27	FOS	chr4:68799523-68799825	MCF10A-Er-Src	breast:	n/a	chr4:68799670-68799679
28	FOS	chr4:68796859-68797351	MCF10A-Er-Src	breast:	n/a	chr4:68797085-68797092 chr4:68797084-68797093 chr4:68797084-68797092 chr4:68797083-68797092
29	FOS	chr4:68795114-68795590	MCF10A-Er-Src	breast:	n/a	chr4:68795296-68795305 chr4:68795410-68795420
30	FOS	chr4:68795144-68795590	MCF10A-Er-Src	breast:	n/a	chr4:68795296-68795305 chr4:68795410-68795420
31	FOS	chr4:68799523-68799790	MCF10A-Er-Src	breast:	n/a	chr4:68799670-68799679
32	FOS	chr4:68799563-68799759	MCF10A-Er-Src	breast:	n/a	chr4:68799670-68799679
33	FOS	chr4:68794176-68794607	MCF10A-Er-Src	breast:	n/a	chr4:68794319-68794328
34	FOS	chr4:68794141-68794602	MCF10A-Er-Src	breast:	n/a	chr4:68794319-68794328
35	FOS	chr4:68796933-68797350	MCF10A-Er-Src	breast:	n/a	chr4:68797085-68797092 chr4:68797084-68797093 chr4:68797084-68797092 chr4:68797083-68797092
36	FOS	chr4:68795064-68795826	MCF10A-Er-Src	breast:	n/a	chr4:68795296-68795305 chr4:68795410-68795420
37	FOS	chr4:68796937-68797293	MCF10A-Er-Src	breast:	n/a	chr4:68797085-68797092 chr4:68797084-68797093 chr4:68797084-68797092 chr4:68797083-68797092
38	FOS	chr4:68795014-68795873	MCF10A-Er-Src	breast:	n/a	chr4:68795296-68795305 chr4:68795410-68795420
39	FOSL1	chr4:68795061-68795651	HCT-116	colon:	n/a	chr4:68795296-68795305 chr4:68795410-68795420
40	FOSL1	chr4:68794198-68794644	HCT-116	colon:	n/a	chr4:68794319-68794328
41	FOXA1	chr4:68794489-68794740	HepG2	liver:	n/a	chr4:68794641-68794656 chr4:68794663-68794678
42	FOXA1	chr4:68794560-68794794	T-47D	breast:	n/a	chr4:68794641-68794656 chr4:68794663-68794678
43	FOXA2	chr4:68794555-68794727	HepG2	liver:	n/a	n/a
44	FOXM1	chr4:68794210-68794723	MCF-7	breast:	n/a	n/a
45	FOXM1	chr4:68794212-68794781	MCF-7	breast:	n/a	n/a
46	GATA3	chr4:68794219-68795018	MCF-7	breast:	n/a	chr4:68794473-68794485 chr4:68794997-68795010 chr4:68794471-68794487 chr4:68794475-68794482 chr4:68794414-68794421 chr4:68794475-68794484 chr4:68794474-68794484
47	GATA3	chr4:68794361-68794735	MCF-7	breast:	n/a	chr4:68794473-68794485 chr4:68794471-68794487 chr4:68794475-68794482 chr4:68794414-68794421 chr4:68794475-68794484 chr4:68794474-68794484
48	GATA3	chr4:68795623-68796017	MCF-7	breast:	n/a	n/a
49	GATA3	chr4:68794260-68794925	MCF-7	breast:	n/a	chr4:68794473-68794485 chr4:68794471-68794487 chr4:68794475-68794482 chr4:68794414-68794421 chr4:68794475-68794484 chr4:68794474-68794484
50	GATA3	chr4:68794106-68794953	MCF-7	breast:	n/a	chr4:68794473-68794485 chr4:68794471-68794487 chr4:68794475-68794482 chr4:68794414-68794421 chr4:68794475-68794484 chr4:68794474-68794484

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:68801145-68801195	HRCEpiC	kidney:	n/a
2	chr4:68801145-68801195	HRCEpiC	kidney:	n/a
3	chr4:68829101-68829151	ECC-1	luminal epithelium:	n/a
4	chr4:68830227-68830277	ECC-1	luminal epithelium:	n/a
5	chr4:68830227-68830277	GM06990	blood:	n/a
6	chr4:68829101-68829151	HCM	heart:	n/a
7	chr4:68829101-68829151	ProgFib	skin:	n/a
8	chr4:68829101-68829151	RPTEC	kidney:	n/a
9	chr4:68801145-68801195	GM19239	blood:	n/a
10	chr4:68829101-68829151	HAEpiC	amniotic membrane:	n/a
11	chr4:68829101-68829151	HCT-116	colon:	n/a
12	chr4:68830227-68830277	HCT-116	colon:	n/a
13	chr4:68830227-68830277	NHBE	bronchial:	n/a
14	chr4:68801145-68801195	PrEC	prostate:	n/a
15	chr4:68801145-68801195	SK-N-MC	brain:	n/a
16	chr4:68801145-68801195	GM12891	blood:	n/a
17	chr4:68830227-68830277	BE2_C	brain:	n/a
18	chr4:68829101-68829151	ovcar-3	ovarian:	n/a
19	chr4:68801145-68801195	HEK293	kidney:	embryo
20	chr4:68830227-68830277	AG10803	skin:	n/a
21	chr4:68801145-68801195	HepG2	liver:	n/a
22	chr4:68830227-68830277	LNCaP	prostate:	n/a
23	chr4:68830227-68830277	HEEpiC	esophagus:	n/a
24	chr4:68829101-68829151	A549	lung:	n/a
25	chr4:68830227-68830277	SK-N-MC	brain:	n/a
26	chr4:68830227-68830277	NHDF-neo	bronchial:	n/a
27	chr4:68829101-68829151	GM12892	blood:	n/a
28	chr4:68801145-68801195	HCPEpiC	choroid plexus:	n/a
29	chr4:68829101-68829151	SAEC	small airway:	n/a
30	chr4:68829101-68829151	AG09309	skin:	n/a
31	chr4:68801145-68801195	HAEpiC	amniotic membrane:	n/a
32	chr4:68830227-68830277	HUVEC	blood vessel:	n/a
33	chr4:68801145-68801195	GM06990	blood:	n/a
34	chr4:68829101-68829151	NHDF-neo	bronchial:	n/a
35	chr4:68829101-68829151	PrEC	prostate:	n/a
36	chr4:68829101-68829151	Jurkat	blood:	n/a
37	chr4:68829101-68829151	HMEC	breast:	n/a
38	chr4:68829101-68829151	GM12891	blood:	n/a
39	chr4:68830227-68830277	HPAEpiC	pulmonary alveolar:	n/a
40	chr4:68801145-68801195	RPTEC	kidney:	n/a
41	chr4:68801145-68801195	NB4	blood:	n/a
42	chr4:68830227-68830277	Jurkat	blood:	n/a
43	chr4:68830227-68830277	HRE	kidney:	n/a
44	chr4:68830227-68830277	HepG2	liver:	n/a
45	chr4:68830227-68830277	HMEC	breast:	n/a
46	chr4:68801145-68801195	HMEC	breast:	n/a
47	chr4:68829101-68829151	AG04449	skin:	fetal
48	chr4:68829101-68829151	GM19239	blood:	n/a
49	chr4:68801145-68801195	AG09309	skin:	n/a
50	chr4:68830227-68830277	GM12878	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:68801891..68804770-chr4:68805510..68808424,3	K562	blood:
2	chr4:68794213..68794935-chr4:69590279..69590859,2	MCF-7	breast:
3	chr4:68782641..68784982-chr4:68793433..68796175,2	MCF-7	breast:
4	chr4:68794156..68795825-chr4:69317354..69319516,2	MCF-7	breast:
5	chr4:68565498..68567091-chr4:68824885..68827731,2	K562	blood:
6	chr4:68796679..68798591-chr4:68806253..68807881,2	MCF-7	breast:
7	chr4:68802859..68804770-chr4:68805510..68807108,2	K562	blood:
8	chr4:68794052..68794960-chr4:69050850..69051709,2	MCF-7	breast:
9	chr4:68798924..68801314-chr4:68932123..68934294,2	MCF-7	breast:
10	chr4:68787068..68789277-chr4:68795494..68798392,2	MCF-7	breast:
11	chr4:68794355..68794979-chr4:68995102..68995843,2	MCF-7	breast:
12	chr4:68791805..68794624-chr4:68798478..68800793,2	K562	blood:
13	chr4:68794694..68797024-chr4:69366841..69368465,2	MCF-7	breast:
14	chr4:68794060..68794853-chr4:68904568..68905079,2	MCF-7	breast:
15	chr4:68796679..68798591-chr4:68806253..68807881,2	MCF-7	breast:
16	chr4:68802859..68804770-chr4:68805510..68807108,2	K562	blood:
17	chr4:68791805..68794624-chr4:68798478..68800793,2	K562	blood:
18	chr4:68801891..68804770-chr4:68805510..68808424,3	K562	blood:
19	chr4:68788622..68791120-chr4:68792670..68794501,2	MCF-7	breast:
20	chr4:68793797..68796085-chr4:69232793..69234726,2	MCF-7	breast:
21	chr4:68794157..68794866-chr4:69050816..69051359,2	MCF-7	breast:
22	chr4:68577504..68578308-chr4:68794030..68794919,2	MCF-7	breast:
23	chr4:68788496..68791205-chr4:68791799..68795295,5	MCF-7	breast:

Variant related genes	Relation type
TMPRSS11A	TF binding region
TMPRSS11A	CpG island
ENSG00000248049	chromatin interactions
ENSG00000198092	chromatin interactions
ENSG00000033178	chromatin interactions

Extended variants
information (count: 1203 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:1203 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs564642819	chr4:68793591-68793592	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs533077146	chr4:68793617-68793618	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs546336220	chr4:68793621-68793622	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs566465363	chr4:68793632-68793633	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs377544109	chr4:68793694-68793695	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs529542193	chr4:68793731-68793732	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs28722166	chr4:68793741-68793742	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs4429773	chr4:68793784-68793785	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs192835744	chr4:68793822-68793823	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs79765239	chr4:68793824-68793825	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs577381748	chr4:68793825-68793826	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs4515215	chr4:68793846-68793847	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs539927988	chr4:68793851-68793852	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs553240406	chr4:68793856-68793857	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs533613702	chr4:68793871-68793872	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs573281197	chr4:68793912-68793913	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs353153	chr4:68793913-68793914	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs370440265	chr4:68793921-68793922	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs540249086	chr4:68793931-68793932	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs139835092	chr4:68793964-68793965	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs182536523	chr4:68794000-68794001	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs564677150	chr4:68794011-68794012	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs145380021	chr4:68794015-68794016	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs353152	chr4:68794034-68794035	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs560030771	chr4:68794043-68794044	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs353151	chr4:68794044-68794045	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs548728143	chr4:68794071-68794072	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs114396367	chr4:68794076-68794077	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs537761781	chr4:68794117-68794118	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs551215911	chr4:68794161-68794162	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs571206686	chr4:68794172-68794173	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs533790845	chr4:68794190-68794191	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs553920725	chr4:68794297-68794298	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs149854677	chr4:68794408-68794409	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs187185529	chr4:68794415-68794416	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs551491208	chr4:68794483-68794484	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs535917184	chr4:68794489-68794490	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs28541914	chr4:68794529-68794530	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs575671363	chr4:68794552-68794553	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs17639952	chr4:68794553-68794554	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs192024326	chr4:68794651-68794652	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs72645805	chr4:68794660-68794661	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs353150	chr4:68794715-68794716	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs372337582	chr4:68794719-68794720	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs17088775	chr4:68794770-68794771	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs184433824	chr4:68794789-68794790	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs78223682	chr4:68794834-68794835	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs567368903	chr4:68794853-68794854	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs190517229	chr4:68794862-68794863	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs193113470	chr4:68794889-68794890	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:83)

Disease	PMID	Source
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Medulloblastoma	21979893	CNVD
Neuroblastoma	18923191	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Non-small cell lung cancer	21829676	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Lung cancer	18438408	CNVD
Breast cancer	17603634	CNVD
Glioblastoma multiforme	21922591	CNVD
Parkinson disease	21956041	CNVD
Mental retardation	20522426	CNVD
delayed speech	20522426	CNVD
growth disorder	20522426	CNVD
Hepatocellular carcinoma	16750200	CNVD
Myxofibrosarcoma	16751306	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Parkinson disease	18923514	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	CNVD
Breast cancer	16272173	CNVD
Multiple myeloma	16616336	CNVD
Colorectal cancer	19359472	CNVD
Malignant mesothelioma	18160781	CNVD
Medulloblastoma	18056178	CNVD
Multiple myeloma	17077331	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Oral squamous cell carcinoma	17134496	CNVD
4q-syndrome	17576883	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Muscular dystrophy	21149563	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Cervical cancer	21062161	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Colorectal cancer	16272173	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Lung cancer	19208797	CNVD
small cell lung cancer	20016488	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16573809	CNVD
Osteoporosis	18992858	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Breast cancer	20369283	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Myelodysplastic syndrome	21251322	CNVD
Multiple myeloma	17550852	CNVD
Graft versus host disease	20877625	CNVD
Breast cancer	21990379	CNVD
Myelofibrosis	22110671	CNVD
Osteoporosis	20877625	CNVD
Osteoporosis	19737800	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Glioblastoma multiforme	21138945	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:82 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:68792600-68793600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr4:68793200-68794400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
3	chr4:68793400-68806600	Weak transcription	Esophagus	oesophagus
4	chr4:68793600-68794800	Enhancers	Primary hematopoietic stem cells	blood
5	chr4:68793600-68799800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr4:68794000-68794800	Enhancers	Primary hematopoietic stem cells short term culture	blood
7	chr4:68794000-68794800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
8	chr4:68794000-68794800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr4:68794200-68796400	Enhancers	Hela-S3	cervix
10	chr4:68794200-68799000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
11	chr4:68794400-68796000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr4:68794400-68796000	Enhancers	HMEC	breast
13	chr4:68794400-68796200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
14	chr4:68794400-68797800	Enhancers	NHEK	skin
15	chr4:68794600-68795200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
16	chr4:68794800-68799200	Weak transcription	Primary hematopoietic stem cells	blood
17	chr4:68794800-68799400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
18	chr4:68794800-68799400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
19	chr4:68794800-68799800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
20	chr4:68795200-68800000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
21	chr4:68796000-68799400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
22	chr4:68796200-68797400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr4:68797400-68797800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
24	chr4:68797800-68800200	Weak transcription	NHEK	skin
25	chr4:68797800-68800400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
26	chr4:68798600-68802000	Enhancers	Dnd41	blood
27	chr4:68798800-68799000	Enhancers	HUES64 Cell Line	embryonic stem cell
28	chr4:68799000-68799400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
29	chr4:68799000-68800000	Weak transcription	HUES64 Cell Line	embryonic stem cell
30	chr4:68799200-68802200	Enhancers	Primary hematopoietic stem cells	blood
31	chr4:68799400-68799600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
32	chr4:68799400-68800000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
33	chr4:68799400-68800200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
34	chr4:68799400-68801000	Enhancers	ES-I3 Cell Line	embryonic stem cell
35	chr4:68799400-68801000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
36	chr4:68799600-68800000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
37	chr4:68799800-68801000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr4:68799800-68801000	Enhancers	iPS-20b Cell Line	embryonic stem cell
39	chr4:68799800-68801000	Enhancers	Fetal Heart	heart
40	chr4:68799800-68801200	Enhancers	Primary hematopoietic stem cells short term culture	blood
41	chr4:68800000-68800600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
42	chr4:68800000-68800800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
43	chr4:68800000-68801000	Enhancers	iPS-18 Cell Line	embryonic stem cell
44	chr4:68800000-68801200	Enhancers	HUES64 Cell Line	embryonic stem cell
45	chr4:68800000-68801200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
46	chr4:68800200-68800400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
47	chr4:68800200-68800800	Enhancers	HUES48 Cell Line	embryonic stem cell
48	chr4:68800200-68800800	Enhancers	iPS-15b Cell Line	embryonic stem cell
49	chr4:68800200-68800800	Enhancers	NHEK	skin
50	chr4:68800200-68801200	Enhancers	Fetal Intestine Small	intestine

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